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Structural basis for recognition of phosphodiester-containing lysosomal enzymes by the cation-independent mannose 6-phosphate receptor

Proceedings of the National Academy of Sciences - PNAS, 2010-07, Vol.107 (28), p.12493-12498

2010

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Cation-independent mannose 6-phosphate receptor: a composite of distinct phosphomannosyl binding sites

The Journal of biological chemistry, 2009-12, Vol.284 (50), p.35215-35226

2009

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Domain 5 of the Cation-Independent Mannose 6-Phosphate Receptor Preferentially Binds Phosphodiesters (Mannose 6-Phosphate N-Acetylglucosamine Ester)

Biochemistry (Easton), 2007-11, Vol.46 (44), p.12604-12617

2007

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Optimization of cytochrome P4502D6 (CYP2D6) phenotype assignment using a genotyping algorithm based on allele frequency data

Pharmacogenetics and genomics, 1999-12, Vol.9 (6), p.669-682

1999

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Cytochrome P450 Involvement in the biotransformation of cisapride and racemic norcisapride in vitro: differential activity of individual human CYP3A isoforms

Drug metabolism and disposition, 2001-12, Vol.29 (12), p.1548

2001

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Cation-independent Mannose 6-Phosphate Receptor

The Journal of biological chemistry, 2009-12, Vol.284 (50), p.35215-35226

2009

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Potent inhibition of cytochrome P-450 2D6-mediated dextromethorphan O-demethylation by terbinafine

Drug metabolism and disposition, 1999-07, Vol.27 (7), p.770

1999

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Investigation of terbinafine as a CYP2D6 inhibitor in vivo

Clinical pharmacology and therapeutics, 1999-05, Vol.65 (5), p.465-472

1999

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Structural features of mammalian gonadotropins

Molecular and cellular endocrinology, 1996-12, Vol.125 (1), p.3-19

1996

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Glycosylated equine prolactin and its carbohydrate moiety

Journal of protein chemistry, 1996-07, Vol.15 (5), p.413-426

1996

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Carbohydrate Analysis of Glycoprotein Hormones

Methods (San Diego, Calif.), 2000-05, Vol.21 (1), p.15-39

2000

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Negative influence of O-linked oligosaccharides of high molecular weight equine chorionic gonadotropin on its luteinizing hormone and follicle-stimulating hormone receptor-binding activities

Endocrinology (Philadelphia), 1996-06, Vol.137 (6), p.2530-2542

1996

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Hormone-Specific Inhibitory Influence of α-Subunit Asn56 Oligosaccharide on In Vitro Subunit Association and Follicle-Stimulating Hormone Receptor Binding of Equine Gonadotropins1

Biology of reproduction, 1998-02, Vol.58 (2), p.458-469

1998

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Optimization of cytochrome P4502D6 (CYP2D6) phenotype assignment using a genotyping algorithm based on allele frequency data

Pharmacogenetics (London), 1999-12, Vol.9 (6), p.669-682

1999

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M021: rhGAA with optimal glycosylation profile containing very high levels of bis-phosphorylated N-glycans clears accumulated glycogen and rapidly normalizes muscle strength in treated Pompe disease mice

Molecular genetics and metabolism, 2023-02, Vol.138 (2), p.107125, Article 107125

2023

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Role of TGF‐β in a Mouse Model of High Turnover Renal Osteodystrophy

Journal of bone and mineral research, 2014-05, Vol.29 (5), p.1141-1157

2014

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Hyaluronan Biosynthesis by Class I Streptococcal Hyaluronan Synthases Occurs at the Reducing End

The Journal of biological chemistry, 2005-04, Vol.280 (13), p.13012-13018

2005

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Co-administration of the pharmacological chaperone AT2221 with a proprietary recombinant human acid alfa-glucosidase leads to greater plasma exposure and substrate reduction compared to alglucosidase alfa

Molecular genetics and metabolism, 2016-02, Vol.117 (2), p.S66-S67

2016

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Combined phenotypic assessment of CYP1A2, CYP2C19, CYP2D6, CYP3A, N‐acetyltransferase‐2, and xanthine oxidase with the “Cooperstown cocktail”

Clinical pharmacology and therapeutics, 2000-10, Vol.68 (4), p.375-383

2000

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Role of TGF-[beta] in a Mouse Model of High Turnover Renal Osteodystrophy

Journal of bone and mineral research, 2014-05, Vol.29 (5), p.1141

2014

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Effect of fluvoxamine therapy on the activities of CYP1A2, CYP2D6, and CYP3A as determined by phenotyping

Clinical pharmacology and therapeutics, 1998-09, Vol.64 (3), p.257-268

1998

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Pharmacokinetics and pharmacodynamics following low dose TSH administration in aged ovariectomized rats

The FASEB journal, 2007-04, Vol.21 (5), p.A432-A432

2007

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Quantitation of three‐month intraindividual variability and influence of sex and menstrual cycle phase on CYP1A2, N‐acetyltransferase‐2, and xanthine oxidase activity determined with caffeine phenotyping

Clinical pharmacology and therapeutics, 1998-05, Vol.63 (5), p.540-551

1998

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Dose dependency of dextromethorphan for cytochrome P450 2D6 (CYP2D6) phenotyping

Clinical pharmacology and therapeutics, 1999-11, Vol.66 (5), p.535-541

1999

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Quantification of intraindividual variability and the influence of menstrual cycle phase on CYP2D6 activity as measured by dextromethorphan phenotyping

Pharmacogenetics (London), 1998-10, Vol.8 (5), p.403-410

1998

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Structural basis for recognition of phosphodiester-containing lysosomal enzymes by the cation-independent mannose 6-phosphate receptor

Cation-independent mannose 6-phosphate receptor: a composite of distinct phosphomannosyl binding sites

Domain 5 of the Cation-Independent Mannose 6-Phosphate Receptor Preferentially Binds Phosphodiesters (Mannose 6-Phosphate N-Acetylglucosamine Ester)

Optimization of cytochrome P4502D6 (CYP2D6) phenotype assignment using a genotyping algorithm based on allele frequency data

Cytochrome P450 Involvement in the biotransformation of cisapride and racemic norcisapride in vitro: differential activity of individual human CYP3A isoforms

Cation-independent Mannose 6-Phosphate Receptor

Potent inhibition of cytochrome P-450 2D6-mediated dextromethorphan O-demethylation by terbinafine

Investigation of terbinafine as a CYP2D6 inhibitor in vivo

Structural features of mammalian gonadotropins

Glycosylated equine prolactin and its carbohydrate moiety

Carbohydrate Analysis of Glycoprotein Hormones

Negative influence of O-linked oligosaccharides of high molecular weight equine chorionic gonadotropin on its luteinizing hormone and follicle-stimulating hormone receptor-binding activities

Hormone-Specific Inhibitory Influence of α-Subunit Asn56 Oligosaccharide on In Vitro Subunit Association and Follicle-Stimulating Hormone Receptor Binding of Equine Gonadotropins1

Optimization of cytochrome P4502D6 (CYP2D6) phenotype assignment using a genotyping algorithm based on allele frequency data

M021: rhGAA with optimal glycosylation profile containing very high levels of bis-phosphorylated N-glycans clears accumulated glycogen and rapidly normalizes muscle strength in treated Pompe disease mice

Role of TGF‐β in a Mouse Model of High Turnover Renal Osteodystrophy

Hyaluronan Biosynthesis by Class I Streptococcal Hyaluronan Synthases Occurs at the Reducing End

Co-administration of the pharmacological chaperone AT2221 with a proprietary recombinant human acid alfa-glucosidase leads to greater plasma exposure and substrate reduction compared to alglucosidase alfa

Combined phenotypic assessment of CYP1A2, CYP2C19, CYP2D6, CYP3A, N‐acetyltransferase‐2, and xanthine oxidase with the “Cooperstown cocktail”

Role of TGF-[beta] in a Mouse Model of High Turnover Renal Osteodystrophy

Effect of fluvoxamine therapy on the activities of CYP1A2, CYP2D6, and CYP3A as determined by phenotyping

Pharmacokinetics and pharmacodynamics following low dose TSH administration in aged ovariectomized rats

Quantitation of three‐month intraindividual variability and influence of sex and menstrual cycle phase on CYP1A2, N‐acetyltransferase‐2, and xanthine oxidase activity determined with caffeine phenotyping

Dose dependency of dextromethorphan for cytochrome P450 2D6 (CYP2D6) phenotyping

Quantification of intraindividual variability and the influence of menstrual cycle phase on CYP2D6 activity as measured by dextromethorphan phenotyping

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